Trial Profile
A Multicenter, Randomized, Double-Blind, Placebo-Controlled, 12-Week Study to Evaluate the Efficacy and Safety of Extended Release (ER) Niacin/Laropiprant When Added to Ongoing Lipid-Modifying Therapy in Dyslipidemic Patients.
Status:
Discontinued
Phase of Trial:
Phase IV
Latest Information Update: 10 Aug 2019
Price :
$35
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At a glance
- Drugs Niacin/laropiprant (Primary)
- Indications Dyslipidaemias
- Focus Therapeutic Use
- Sponsors Merck Sharp & Dohme
- 10 Aug 2019 Status changed from recruiting to discontinued.
- 04 Jul 2012 Actual initiation date changed from 30 Mar 2009 to 30 May 2008 as reported by European Clinical Trials Database.
- 04 Jul 2012 Planned end date changed from 30 Jun 2010 to 30 Aug 2009 as reported by European Clinical Trials Database.